KaVo INTRAcompact contra-angle 0768 LHC Instructions For Use Manual page 15

Setup methods according to DIN EN ISO 17664
Setup methods according to DIN EN ISO 17664
Setup methods according to DIN EN ISO 17664
Setup methods according to DIN EN ISO 17664
7 7 .6 P P ackaging
Note
The sterilisation bag must be large enough for the instrument so that the
bag is not stretched.
The quality and use of the sterilised product packaging must satisfy ap‐
plicable standards and be suitable for the sterilisation procedure.
▶ Individually weld the medical device in the sterilised item packaging
(such as KaVo STERIclave bags M M at. no. 0.411.9912)!
7 7 .7 S S terilisation
Sterilisation in a steam steriliser (autoclave) in accordance with EN 13060/
ISO 17665-1 (e.g. KaVo STERIclave B 2200 / 2200 P)
CAUTION
Premature wear and malfunctions from improper servicing and care.
Reduced product life.
▶ Before each sterilisation cycle, service the medical device with KaVo
care products.
CAUTION
Contact corrosion due to moisture.
Damage to product.
▶ Immediately remove the product from the steam steriliser after the
sterilisation cycle!
The KaVo medical device has a maximum temperature resistance up to
138 ℃ (280.4 °F).
(Depending on the available autoclave,) select a suitable procedure from
the following sterilisation processes:
▪ Autoclave with three times initial vacuum:
– at least 3 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4
°F)
▪ Autoclave using the gravitation method:
– at least 10 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4
°F) or alternatively
– at least 60 minutes at 121 °C -1 °C / +4 °C (250 °F -1.6 °F / +7.4
°F)
▶ Use according to the manufacturer's Instructions for Use.
7 7 .8 S S torage
Prepared products must be stored, protected from germs (as far as possi‐
ble) and dust, in a dry, dark, cool room.
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